01 4DEXTROAMPHETAMINE
02 5ESTRADIOL
03 2ESTRADIOL; NORETHINDRONE ACETATE
04 4FENTANYL
05 3LIDOCAINE
06 3LITHIUM CARBONATE
07 4METHYLPHENIDATE
08 3NITROGLYCERIN
01 2JDS PHARMS
02 14NOVEN
03 11NOVEN PHARMS INC
04 1NOVEN THERAP
01 1CAPSULE;ORAL
02 1FILM, EXTENDED RELEASE;BUCCAL
03 15FILM, EXTENDED RELEASE;TRANSDERMAL
04 3Film, Extended Release; Transdermal
05 2PATCH;TOPICAL
06 4SYSTEM;TRANSDERMAL
07 1TABLET, EXTENDED RELEASE;ORAL
08 1TABLET;ORAL
01 10.025MG/24HR
02 10.0375MG/24HR
03 10.05MG/24HR
04 10.05MG/24HR;0.14MG/24HR
05 10.05MG/24HR;0.25MG/24HR
06 10.075MG/24HR
07 10.1MG/24HR
08 10.2MG/HR
09 10.4MG/HR
10 10.6MG/HR
11 1100MCG/HR
12 110MG/9HR (1.1MG/HR)
13 113.5MG/9HR
14 115MG/9HR (1.6MG/HR)
15 118MG/9HR
16 120MG/9HR (2.2MG/HR)
17 123MG/PATCH
18 125MCG/HR
19 2300MG
20 130MG/9HR (3.3MG/HR)
21 14.5MG/9HR
22 1450MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 146.1MG/PATCH
24 15%
25 150MCG/HR
26 175MCG/HR
27 19MG/9HR
01 28USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SYSTEM;TRANSDERMAL
Brand Name : XELSTRYM
Dosage Strength : 4.5MG/9HR
Packaging :
Approval Date : 2022-03-22
Application Number : 215401
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SYSTEM;TRANSDERMAL
Brand Name : XELSTRYM
Dosage Strength : 9MG/9HR
Packaging :
Approval Date : 2022-03-22
Application Number : 215401
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SYSTEM;TRANSDERMAL
Brand Name : XELSTRYM
Dosage Strength : 13.5MG/9HR
Packaging :
Approval Date : 2022-03-22
Application Number : 215401
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SYSTEM;TRANSDERMAL
Brand Name : XELSTRYM
Dosage Strength : 18MG/9HR
Packaging :
Approval Date : 2022-03-22
Application Number : 215401
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FILM, EXTENDED RELEASE;T...
Brand Name : MINIVELLE
Dosage Strength : 0.0375MG/24HR
Packaging :
Approval Date : 2012-10-29
Application Number : 203752
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FILM, EXTENDED RELEASE;T...
Brand Name : MINIVELLE
Dosage Strength : 0.075MG/24HR
Packaging :
Approval Date : 2012-10-29
Application Number : 203752
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FILM, EXTENDED RELEASE;T...
Brand Name : MINIVELLE
Dosage Strength : 0.05MG/24HR
Packaging :
Approval Date : 2012-10-29
Application Number : 203752
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FILM, EXTENDED RELEASE;T...
Brand Name : MINIVELLE
Dosage Strength : 0.1MG/24HR
Packaging :
Approval Date : 2012-10-29
Application Number : 203752
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FILM, EXTENDED RELEASE;T...
Brand Name : MINIVELLE
Dosage Strength : 0.025MG/24HR
Packaging :
Approval Date : 2014-09-23
Application Number : 203752
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ESTRADIOL; NORETHINDRONE ACETATE
Dosage Form : FILM, EXTENDED RELEASE;T...
Brand Name : COMBIPATCH
Dosage Strength : 0.05MG/24HR;0.14MG/24H...
Packaging :
Approval Date : 1998-08-07
Application Number : 20870
Regulatory Info : RX
Registration Country : USA
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